Abstract
Plasma cells, the terminal effectors of the B lymphoid lineage, are responsible for the humoral arm of adaptive immunity. Their differentiation from B cells entails a profound cellular reshaping inherently associated with stress. Autophagy is a conserved adaptive cellular strategy recently implicated in differentiation and immunity. We identified a novel autophagic function in plasma cells. Autophagy restricts the expression of the transcriptional repressor Blimp-1 and immunoglobulins through a selective negative control on the endoplasmic reticulum and its stress signaling response, thereby optimizing energy and viability. As a result, autophagy in vivo sustains antibody responses, and is an essential intrinsic determinant of the bone marrow long-lived plasma cell niche. Here, I discuss several immune and biomedical implications, and experimental issues to be addressed in the near future.
Original language | English |
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Pages (from-to) | 289-295 |
Number of pages | 7 |
Journal | Molecular Immunology |
Volume | 62 |
Issue number | 2 |
DOIs | |
Publication status | Published - Dec 1 2014 |
Keywords
- Antibody
- Atg5
- Autophagy
- B cell
- Blimp-1
- Endoplasmic reticulum
- ER-phagy
- Immunological memory
- Multiple myeloma
- Plasma cell
- Proteostasis
- Reticulophagy
- Ubiquitin
- Unfolded protein response
- XBP-1
ASJC Scopus subject areas
- Molecular Biology
- Immunology